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952 Possible Causes for Jaundice, Mild Anemia, Splenomegaly

  • Hemolytic Anemia

    The existence of a primary form of acquired hemolytic jaundice has been questioned more and FULL TEXT[annals.org] All the children presented with neonatal hemolytic anemia. Beyond the neonatal period, they did not have jaundice or hemolysis, but continued to have mild anemia.[ncbi.nlm.nih.gov] It results in hemolytic anemia and splenomegaly.[icd9data.com]

  • Thalassemia

    Diagnostic methods Diagnosis is suspected in infants younger than 2 years of age with severe microcytic anemia, mild jaundice and hepatosplenomegaly.[orpha.net] Mild anemia can make you feel tired. Mild anemia caused by alpha thalassemia trait might be mistaken for iron-deficiency anemia.[web.archive.org] Approach to the adult patient with splenomegaly and other splenic disorders. . Accessed June 14, 2016. Splenomegaly. Merck Manual Professional Version. .[mayoclinic.org]

  • Hereditary Spherocytosis

    This case also highlights the fact that physicians should consider concomitant hemolytic disease in patients in whom jaundice and infections that rarely cause jaundice coexist[ncbi.nlm.nih.gov] A 27-year-old Nigerian woman presented with mild anemia, jaundice, splenomegaly and a history of multiple blood transfusion.[ncbi.nlm.nih.gov] Due to the membrane defect, there is increased fragility, hemolytic anemia, marked splenomegaly and hyperbilirubinemia.[ncbi.nlm.nih.gov]

  • Alpha-Thalassemia

    Alpha-thalassemia Alpha-thalassemia inheritance pattern Specialty Hematology Symptoms Jaundice, Fatigue Anie KA, Massaglia P (March 2014).[en.wikipedia.org] The heterozygous form may be asymptomatic or marked by mild anemia. β-thalassemia ( beta-thalassemia ) that caused by diminished synthesis of beta chains of hemoglobin.[medical-dictionary.thefreedictionary.com] BACKGROUND: Hereditary spherocytosis (HS) is a common inherited hemolytic anemia characterized by heterogeneous clinical presentations with variable degrees of anemia, jaundice, splenomegaly[ncbi.nlm.nih.gov]

  • Cooley's Anemia

    Children develop life-threatening anemia, have failure to thrive, and may develop jaundice.[secure.ssa.gov] People with Cooley's anemia make less hemoglobin and fewer circulating red blood cells than normal, which results in mild or severe anemia.[blood.emedtv.com] Splenomegaly, episodes of jaundice and roentgenologic evidence of bone involvement were prominent features.[jamanetwork.com]

  • Congenital Hemolytic Anemia

    jaundice (yellowing) and splenomegaly (enlargement of the spleen).[medicinenet.com] anemia.[ncbi.nlm.nih.gov] Children with massive splenomegaly had similar outcomes compared with children without massive splenomegaly.[ncbi.nlm.nih.gov]

  • Congenital Dyserythropoietic Anemia

    , Neonatal/diagnosis Jaundice, Neonatal/etiology Jaundice, Neonatal/therapy Microscopy, Electron Phototherapy Pregnancy[ncbi.nlm.nih.gov] All patients presented with mild anemia, marked hyperbilirubinemia and splenomegaly.[ncbi.nlm.nih.gov] CDA I patients have a moderate macrocytic anemia with frequent splenomegaly and occasional hepatomegaly.[orpha.net]

  • Infectious Mononucleosis

    We report a case of infectious mononucleosis in a 72-year old jaundiced gentleman with ferritin level of 2438 that normalised on clinical improvement.[ncbi.nlm.nih.gov] anemia, neutropenia, and thrombocytopenia BSR CRP Transaminases Note: Pfeiffer’s gland cells are characterized by a basophilic vacuole in the cytoplasm and eccentrically[lecturio.com] Clinical estimates of splenomegaly are fallible.[ncbi.nlm.nih.gov]

  • Haemoglobin E Disease

    While evaluating the patients of jaundice, we came across two cases of hemoglobin E (Hb E) disorders.[ijpmonline.org] Homozygotes display mild hemolytic anemia and splenomegaly (enlarged spleen). The HbCSpr trait is asymptomatic.[wikilectures.eu] There were no signs of splenomegaly.[nejm.org]

  • Pyruvate Kinase Deficiency

    Pyruvate kinase deficiency may cause pregnancy-associated jaundice.[ncbi.nlm.nih.gov] Patients presenting with hemolytic anemia, either severe or mild hemolytic anemia, should be screened for PKD in the first year of life.[ncbi.nlm.nih.gov] She is doing well with mild splenomegaly.[ncbi.nlm.nih.gov]

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